TURION) is seeking a CAD Manager / Document Control Specialist to join our team in Irvine, CA. CM & Engineering Document Control Assistance. Drawing & Engineering Document Checking with high GD&T proficiency. ...
The Document Automation Specialist will enhance and maintain the document automation systems for all divisions and Health Insurance Exchange (HIX) customers. Document Automation Specialist with LiquidOffice, Autonomy or Teleform. Responsibilities include programming and updating data structures and ...
Ensure document version control and manage regular reviews of controlled documents. Administer and maintain the document control system (e. Veeva Quality Docs) to ensure all documents (SOPs, work instructions, quality manuals) are up-to-date, compliant, and properly managed. Supervise the creation, ...
What you’ll do: Craft and implement robust quality assurance protocols for Wi-Fi HaLow ICs Collaborate with cross-functional teams to proactively address quality-related issues and to ensure seamless alignment in quality control processes Oversee comprehensive testing and validation procedures...
The Trailing Docs Specialist will be responsible for monitoring and forwarding trailing documentation to investors, as well as assisting with scanning and file preparation. Coordinates the tracking, reporting and delivering of trailing documents (deed of trust, title policy, to investors. ...
Ensure document version control and manage regular reviews of controlled documents. Administer and maintain the document control system (e. Veeva Quality Docs) to ensure all documents (SOPs, work instructions, quality manuals) are up-to-date, compliant, and properly managed. Supervise the creation, ...
The Document Control Specialist is responsible for collecting, maintaining, archiving and retrieving all documents necessary to ensure compliance with the company's Procedures and FDA regulations. The Document Control Specialist monitors production operations to ensure that all users have the l...
TURION) is seeking a CAD Manager / Document Control Specialist to join our team in Irvine, CA. CM & Engineering Document Control Assistance. Drawing & Engineering Document Checking with high GD&T proficiency. ...
Ensure document version control and manage regular reviews of controlled documents. Administer and maintain the document control system (e. Veeva Quality Docs) to ensure all documents (SOPs, work instructions, quality manuals) are up-to-date, compliant, and properly managed. Supervise the creation, ...
Irvine based Medical Device Company is looking for a Document Control Specialist. Ensuring new documents and records are consistent with company procedures; reviewing all documentation for accuracy, completeness and consistency in content, format, files and approvals. Administration of the document ...
Are you detail-oriented and passionate about organizing critical information? Staffmark is seeking a skilled Document Control Specialist to join a leading company in Pomona, CA. This role offers the chance to work in a dynamic environment where your expertise in managing documentation will be crucia...
The candidate will report to the Company’s VP of Regulatory and Quality Assurance and will support continuous improvement of the Quality System for clinical, research and development, medical device, and cosmetic divisions. Minimum 2 years of experience in quality control or related field that...
LSA is seeking a Senior Air Quality Specialist with a minimum of 5 years of professional experience and a BS/BA in an engineering, science, environmental, or urban planning field. Ability to perform air quality and greenhouse gas technical analyses in support of California Environmental Quality Act ...
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A paid Product Tester position is perfect for those looking for an entry-level opportunity, flexible or seasonal work, temporary work or part-time work. ...
The Quality Control Clinical Laboratory Specialist position supports the testing and documentation needs of the Quality Control Department during the manufacture and release of company control products. Quality Control Clinical Laboratory Specialist. Job requires working side by side with the Qualit...
The Quality Assurance (QA) Specialist is responsible for performing internal audits, assisting with external audits, overseeing the maintenance of QC records, certifications, review and revision of Standard Operating Procedures (SOPs), training records, Demonstrations of Capability (DOCs), arranging...
Senior Quality Assurance Specialist – Southern California, $90K-$100K. I’m currently partnered with an innovator in connectivity solutions, who are looking for a Senior Quality Assurance Specialist. In this role, you'll play a key part in ensuring compliance with ISO 9001 standards, collaborating ac...
This role is responsible for performing inspection tasks related to in-process, Final and/or Receiving Inspection areas.Perform Inspection on all products within a timely manner.Determine product conformance or non-conformance to drawings.Use SAP to transact product to inventory or to MRB.Write non-...
Excellent opportunity to work for a leading company that provides an amazing culture and growth opportunities.Full time in office- M-F 8am-5pm, Full benefits, $23-$25 per hr depending on experience.Screens voicemails and forwards them to the appropriate entity, department, or employees.Answers/Scree...
If you have a keen eye for detail and enjoy working with data, we encourage you to apply for the Data Entry Clerk position at Sharpcontra today!. As a Data Entry Clerk at Sharpcontra, you will be responsible for accurately entering, maintaining, and updating critical business information into our in...
The Document Control Coordinator I, II, III is responsible for collecting, maintaining, archiving, and retrieving all documents necessary to ensure compliance with company procedures and FDA regulations. The Document Control Specialist monitors production operations to ensure that all users have the...
Quality Control Specialists work as part of a manufacturing team, maintaining records of defective materials and ensuring that defective parts are repaired, re-tested, or pulled from production. Performs, records, and evaluates chemical and physical tests necessary to control production processes or...
POSITION RESPONSIBILITIES Responsibilities include but are not limited to: General administrative assistance with expense reports, document drafting, PowerPoint Presentations, distribution of documents via DocuSign, as needed for non-executive department leaders Overseeing the day-to-day activities ...
Reporting to the Program Director, the Quality Assurance Specialist is responsible for overseeing the functions of quality assurance, quality improvement, and utilization management. Responsibilities include the monitoring of clinical services to assure minimum quality assurance and continuous quali...